US20070066965A1 - Coupling device for medical lines - Google Patents
Coupling device for medical lines Download PDFInfo
- Publication number
- US20070066965A1 US20070066965A1 US10/564,113 US56411304A US2007066965A1 US 20070066965 A1 US20070066965 A1 US 20070066965A1 US 56411304 A US56411304 A US 56411304A US 2007066965 A1 US2007066965 A1 US 2007066965A1
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- US
- United States
- Prior art keywords
- coupling device
- medical line
- coupling
- medical
- diaphragm
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/22—Valves or arrangement of valves
- A61M39/26—Valves closing automatically on disconnecting the line and opening on reconnection thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/10—Tube connectors; Tube couplings
- A61M39/14—Tube connectors; Tube couplings for connecting tubes having sealed ends
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/10—Tube connectors; Tube couplings
- A61M2039/1005—Detection of disconnection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/10—Tube connectors; Tube couplings
- A61M2039/1027—Quick-acting type connectors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/10—Tube connectors; Tube couplings
- A61M2039/1044—Verifying the connection, e.g. audible feedback, tactile feedback, visual feedback, using external light sources
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/22—Valves or arrangement of valves
- A61M39/26—Valves closing automatically on disconnecting the line and opening on reconnection thereof
- A61M2039/267—Valves closing automatically on disconnecting the line and opening on reconnection thereof having a sealing sleeve around a tubular or solid stem portion of the connector
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/10—Tube connectors; Tube couplings
- A61M39/12—Tube connectors; Tube couplings for joining a flexible tube to a rigid attachment
Definitions
- This invention relates to medical lines and, in particular, to a coupling device for connecting two medical lines.
- Medical lines are commonly used to deliver liquids or gases to or from a patient under medical care. Medical fluid lines are used regularly in conjunction with a catheter for the intravenous (IV) delivery of fluids, often including medication. They may also be used for fluid drainage, such as in the case of a urinary catheter. Oxygen lines are often used to deliver oxygen to patients to assist in breathing.
- IV lines Another danger arises in the use of IV lines with newborns and infants. In some cases, infants can be strangled by IV lines if the child becomes entangled in the IV line. This danger also arises in the case of medical lines for the delivery of gases, such as oxygen lines.
- U.S. Pat. Nos. 4,533,349 and 5,637,088 describe connectors or fluid lines that can become detached as a result of a longitudinal pulling force, but detachment results in spillage of fluids and risk of contamination.
- the present invention provides a coupling device with a safety breakaway feature.
- the present invention provides a coupling device having two parts that couple together to connect two medical lines and that automatically decouple when subjected to a predetermined separating force.
- the parts are connected together by way of a detachable snap-fit mechanism that separates when subjected to a predetermined longitudinal force.
- the parts each include a sealing mechanism for sealing the medical lines when the parts are decoupled.
- the present invention provides a coupling device for coupling a patient-side medical line to an equipment-side medical line.
- the coupling device includes a first part adapted to be coupled to a first medical line, the first part having a first passage therethrough to provide fluid communication with the first medical line, the first part including a first seal having a sealed position and an unsealed position, wherein the first seal seals the first medical line when in the sealed position, and a second part adapted to be coupled to a second medical line, the second part having a second passage therethrough to provide fluid communication with the second medical line, the second part including a second seal having a sealed position and an unsealed position, wherein the second seal seals the second medical line when in the sealed position.
- the parts include a connector detachably connecting the first part to the second part in a longitudinal direction, wherein the connector detaches the first and second parts in response to a predetermined force in the longitudinal direction, and wherein each of the seals moves from the sealed position to the unsealed position when the first part is detachably connected to the second part.
- the present invention provides a coupling device for coupling a patient-side medical line to an equipment-side medical line.
- the coupling device includes a first body having a first passage therethrough for coupling to a first medical line, a second body having a second passage therethrough for coupling to a second medical line, and a connection means for detachably connecting the first body-to the second body and providing fluid communication between the first and second medical lines, the connection means disconnecting the first body from the second body in response to a separating force.
- the first body includes a first sealing means for sealing the first medical line and the second body includes a second sealing means for sealing the second medical line when the first and second bodies are disconnected, and for unsealing the first and second medical lines when the first and second bodies are connected.
- the present provides a first adapter for a coupling to a second adapter of a coupling device for coupling a patient-side medical line to an equipment-side medical line, the second adapter having a second body adapted to be coupled to a second medical line.
- the first adapter includes a first body adapted to be coupled to a first medical line, the first body having a first passage therethrough to provide fluid communication with the first medical line, the first body including a first seal having a sealed position and an unsealed position, wherein the first seal seals the first medical line when in the sealed position, the first body including a connector for detachably connecting the first body to the second body in a longitudinal direction, the connector detaching the first and second bodies in response to a predetermined force in the longitudinal direction, wherein each of the seals moves from the sealed position to the unsealed position when the first body is detachably connected to the second body.
- the connector connecting the first part or body to the second part or body includes a snap-fit connector comprising a ridge and a corresponding groove.
- the snap-fit connector comprises a first ridge and a first corresponding groove and a second ridge and a second corresponding groove, wherein the second ridge is selectably engagable with the second corresponding groove so as to allow a user to select between two or more predetermined detachment forces.
- the present invention may include a backflow prevention mechanism or valve, and may include an external med-port.
- FIG. 1 shows a perspective view of a coupling device according to the present invention in a disconnected state
- FIG. 2 shows a cross-sectional view of the coupling device shown in FIG. 1 taken along the line 2 - 2 , with the device in a disconnected state;
- FIG. 3 shows a cross-sectional view of the coupling device shown in FIG. 1 taken along the line 2 - 2 , with the device in a connected state;
- FIG. 4 shows a close-up of the cross-sectional view of one of the diaphragms shown in FIG. 2 ;
- FIG. 5 shows a perspective view of another embodiment of a coupling device according to the present invention, in a disconnected state
- FIG. 6 shows a cross-sectional view of a third embodiment of a coupling device according to the present invention.
- FIG. 7 shows a cross-sectional view of a fourth embodiment of a coupling device according to the present invention.
- FIG. 8 shows a cross-sectional view of a fifth embodiment of a coupling device according to the present invention.
- FIG. 9 shows a cross-sectional view of a sixth embodiment of a coupling device according to the present invention.
- FIGS. 1 and 2 show an embodiment of a coupling device 8 , according to the present invention, in a disconnected state.
- the coupling device 8 includes a first, or female, part 10 and a second, or male, part 12 .
- the parts 10 and 12 each have a forward or proximal end where the two parts 10 and 12 are intended to meet and a back or distal end remote from the forward or proximal end.
- the parts 10 and 12 are adapted to be coupled together at their proximal ends such that they will disengage when subjected to a predetermined longitudinal force, as is further described herein.
- the female part 10 has a cylindrical body 11 having an axial passage 20 extending through the body 11 . At the distal end of the body 11 , the passage 20 is in fluid communication with a fluid line 22 .
- the fluid line 22 may be coupled to the passage 20 through any number of mechanisms for securing the female part 10 to the fluid line 22 , including a barbed connector, crimping, a threaded coupling, a bayonet-style coupling, or a fused connection.
- the part 10 may, in one embodiment, include a bayonet termination for insertion directly into an IV solution bag to provide fluid communication with the passage 22 .
- the female part 10 and/or the male part 12 are not secured directly to the fluid lines.
- the parts 10 , 12 terminate with a connectors which is adapted to be coupled to a corresponding connector on the fluid lines, such as a threaded connector or other known connectors.
- the axial tube 15 Extending forward from the proximal end of the body 11 is an axial tube 15 in fluid communication with the passage 20 .
- the axial tube 15 may be integrally formed with the cylindrical body 11 and terminates in an outer end 17 .
- the outer end 17 of the tube is sealed with a first diaphragm 18 .
- the first diaphragm 18 also seals the passage 20 and the fluid line 22 , thereby preventing fluid flow into or out of the fluid line 22 .
- the diaphragm 18 includes a pre-cut central slit, whereby the diaphragm 18 spreads open at the pre-cut central slit when subjected to sufficient pressure.
- the female part 10 also includes a plurality of forward extending arms 14 arranged at the periphery of the cylindrical body 11 .
- the arms 14 may be integrally formed with the cylindrical body 11 .
- the outer ends of some of the arms 14 include a ridge 16 formed on the inner surface of the arms 14 .
- the ridge 16 may extend circumferentially along the inner surface of one or more arms 14 .
- the arms 14 are resiliently flexible such that when bent radially outwards they will exert an inward radial bias.
- the male part 12 has a cylindrical body 13 having an axial chamber 26 extending longitudinally therethrough.
- a needle 24 (or a tube, a cannula, or other fluid line connector) is coupled to a fluid line 23 and inserted into the axial chamber 26 .
- the needle 24 and fluid line 23 are secured to the cylindrical body. 13 by a threaded coupler 25 having an external thread on its outer surface that cooperates with a corresponding thread formed upon the inner surface of the axial chamber 26 to secure the coupler 25 to the cylindrical body 13 .
- Other mechanisms for coupling the fluid line 23 and needle 24 to the body 13 will be understood by those of ordinary skill in the art, and may include friction fit, adhesives, fusing, etc.
- the male part 12 further includes a tubular sheath 19 disposed within the axial chamber 26 .
- the sheath 19 envelopes the needle 24 and includes a base having an outwardly extending flange 31 .
- the outwardly extending flange 31 is pinched between the cylindrical body 13 and the threaded coupler 25 such that the sheath 19 is in sealed fluid communication with the needle 24 .
- the tip of the sheath 19 terminates in a second diaphragm 28 that seals the tip of the tubular sheath 19 .
- the diaphragm 28 may be formed integrally with the sheath 19 .
- the diaphragm 28 includes a pre-cut central slit, whereby the diaphragm 28 spreads open at the pre-cut central slit when subjected to sufficient pressure.
- the sheath 19 also includes a skirt 21 encircling the tubular portion of the sheath 19 and extending forwardly and outwardly within the axial chamber 26 .
- the outer end of the skirt 21 includes an outwardly extending flange 27 pressed against the front surface of the cylindrical body 13 and held in place with a collar 32 .
- the collar 32 may be push fit into a corresponding annular depression within the front face of the cylindrical body 13 .
- the collar 32 holds the outer end of the skirt 21 in place relative to the cylindrical body 13 .
- the front end of the cylindrical body 13 includes an inwardly tapered outer surface 29 and a circumferential groove 30 .
- the diaphragms 18 and 28 are sealed, preventing any fluid from flowing into or out of the fluid lines 22 and 23 through the passage 20 or the axial chamber 26 .
- FIG. 3 shows the coupling device 8 of FIGS. 1 and 2 in a connected state.
- the inwardly tapered outer surface 29 of the male part 12 fits within the arms 14 of the female part 10 .
- the ridges 16 on the arms 14 are brought into contact with the inwardly tapered outer surface 29 , they are pushed outwards, flexing the arms 14 radially, until the ridges 16 snap into the groove 30 . Accordingly, the two parts 10 and 12 are adapted to snap-fit together.
- the groove 30 and the ridges 16 are rounded, such that they will disengage when subjected to a sufficient longitudinal force.
- This disengagement force may be set at different levels for different uses of the coupling device 8 (e.g. adults versus infants; urinary catheters versus IV lines; etc.). Examples of possible force levels include 1, 5, and 10 lbs.
- Such a force may arise if one of the fluid lines 22 or 23 is caught on an external object or tugged, thereby transferring force into the two parts 10 and 12 . If the force is strong enough, it will cause the rounded edge of the ridges 16 to bear against the rounded edge of the groove 20 , causing the ridges 16 to rise out of the groove 30 against the inward bias of the resiliently flexible arms 14 .
- the extent of the force required to separate the two parts 10 and 12 is configurable by altering the relative shapes of the ridges 16 and the grooves 30 and altering the flexibility of the arms 14 .
- the compacting of the sheath 19 by the axial tube 15 is performed against the resistance of the skirt 21 portion of the sheath 19 .
- the outer end of the skirt 21 remains fixed to the front surface of the cylindrical body 13 of the male part 12 , while the inner end of the skirt 21 where it meets the main body of the sheath 19 is pushed back into the axial chamber 26 .
- This stretching stores a tension in the skirt 21 .
- the tension in the skirt 21 causes it to contract, drawing the body of the sheath 19 back up the axial chamber 26 , causing the sheath 19 to reassume its sealed position enveloping the needle 24 .
- the diaphragm 28 reseals the tip of the sheath 19 , pinching the central slit shut.
- the two diaphragms 28 and 18 When the parts 10 and 12 are fully connected, the two diaphragms 28 and 18 are drawn apart, allowing the needle 24 to enter the axial tube 15 and fluid communication is established between the two fluid lines 22 and 23 .
- the sheath 19 and the two diaphragms 28 and 18 resiliently return to their relaxed and sealed state, thereby sealing the two fluid lines 22 and 23 .
- the coupling device 8 automatically seals the two fluid lines 22 and 23 when the coupling device 8 is purposely or accidentally disconnected, thereby preventing spillage or contamination.
- the coupling device 8 also permits easy connection and disconnection of different fluid lines by providing easy sterilization and resealing capability. This allows for easy connection of a new IV line or new catheter bag to a patient.
- the coupling device 8 may also be used to provide a saline/hep lock or a med port.
- the coupling device 8 Upon disconnection, in one embodiment, the coupling device 8 provides for sufficient backpressure to trigger an alarm on a pump if one is used in association with one of the medical fluid lines.
- FIG. 4 shows a close up of a cross-sectional view of the diaphragm 28 from the male part 12 .
- the following description of the diaphragm 28 may also apply to the diaphragm 18 on the female part 10 .
- the diaphragm 28 seals an inner volume 50 from an external environment 52 . It features a central slit 54 to allow the diaphragm 28 to spread apart when the two parts 10 and 12 are connected together.
- the inner volume 50 contains a fluid under pressure, such that it exerts an outward pressure on the diaphragm 28 .
- the diaphragm 28 features one or more channels 56 formed in the inner surface of the diaphragm 28 and running parallel to the central slit 54 .
- a channel 56 is formed on each side of the central slit 54 .
- the channels 56 each include an angled face 58 extending from the inner surface of the diaphragm 28 into the diaphragm 28 divergently from the central slit 54 .
- the channels 56 and the central slit 54 define two hinged portions 62 of the diaphragm 28 that meet at the central slit 54 .
- the two hinged portions 62 of the diaphragm 28 are each connected to the main part of the diaphragm 28 at a thin point 60 .
- the diaphragms 18 and 28 , and the sheath 19 are all manufactured from silicon.
- suitable materials may include materials such as aliphatic hydrocarbon resins, aliphatic polyester resins, copolymers of olefins and vinyl acetate, olefin-acrylate copolymers, and chlorinated hydrocarbon resins, provided that they are sufficiently resiliently elastic.
- FIG. 5 shows a perspective view of another embodiment of a coupling device 108 , according to the present invention, in a disconnected state.
- the coupling device 108 includes a first, or female, part 10 and a second, or male, part 12 , the parts 10 and 12 each have a forward or proximal end where the two parts 10 and 12 are intended to meet and a back or distal end remote from the forward or proximal end.
- the parts 10 and 12 are adapted to be coupled together at their proximal ends such that they will disengage when subjected to an adjustable predetermined longitudinal force, as is further described below.
- the female part 10 includes a plurality of forward extending arms 14 arranged at the periphery of a cylindrical body 11 .
- One such arm 14 may be marked with an alignment arrow 70 .
- the arms 14 may be integrally formed with the cylindrical body 11 .
- the outer ends of some of the arms 14 include a first ridge 16 and a second ridge 116 formed on the inner surface of the arms 14 .
- the first ridge 16 and the second ridge 116 extend circumferentially along the inner surface of one or more arms 14 .
- the arms 14 are resiliently flexible such that when bent radially outwards they will exert an inward radial bias.
- the male part 12 includes a cylindrical body 13 having an inwardly tapered engagement surface 74 at its proximal end.
- the proximal end of the cylindrical body 13 also includes inwardly sloped clearance surfaces 76 and a circumferential groove 30 .
- the inwardly tapered engagement surfaces 74 define a secondary circumferential groove 72 .
- the secondary circumferential groove 72 is located closer to the proximal end of the cylindrical body 13 than the circumferential groove 30 .
- Cylindrical body 13 may further include first alignment marking 78 , second alignment marking 80 , and third alignment marking 82 .
- the first, second, and third alignment markings 78 , 80 , and 82 may correspond to selectable predetermined longitudinal detachment forces, such as 1, 5, and 10 lbs., when the markings are selectably aligned with the alignment arrow 70 .
- the alignment markings 78 , 80 , and 82 may correspond to different applications for the coupling device 108 , such as infant, pediatric, and adult.
- alignment arrow 70 may be replicated at various intervals around the perimeter of female part 10
- first, second, and third alignment markings 78 , 80 , and 82 may be replicated at various intervals around the perimeter of male part 12 .
- the inwardly tapered engagement surfaces 74 and inwardly sloped clearance surface 76 of the male part 12 fit within the arms 14 of the female part 10 .
- the first ridges 16 on the arms 14 are brought into contact with the inwardly tapered engagement surfaces 74 , preferably at a point between secondary circumferential groove 72 and circumferential groove 30 , they are pushed outwards, flexing the arms 14 radially, until the first ridges 16 snap into the circumferential groove. 30 .
- the extent of the minimum force required to separate the two parts 10 and 12 is configurable by altering the relative shapes of the ridges 16 and the groove 30 and altering the flexibility of the arms 14 , as previously described. Accordingly, the two parts 10 and 12 are adapted to snap-fit together in a first alignment position having a minimum, predetermined separation force.
- the inwardly sloped clearance surfaces 76 may be configured such that the second ridges 116 do not contact or rest against inwardly sloped clearance surfaces 76 when the two parts 10 and 12 have been snap-fit together with alignment arrow 70 aligned with the first alignment marking 78 .
- one of the parts 10 , and 12 may be rotated relative to the other part in a clockwise direction until alignment arrow 70 aligns with the second alignment marking 80 , so as to adjust and increase the predetermined separation force.
- the first ridges 16 on the arms 14 remain engaged with the circumferential groove 30 , ensuring that the female part 10 remains in a fixed longitudinal position relative to male part 12 .
- the second ridges 116 slide into alignment with the secondary circumferential grooves 72 .
- the secondary circumferential groove 72 and the second ridges 116 may be rounded, such that they will disengage when subjected to a sufficient incremental longitudinal separation force.
- the incremental longitudinal separation force may be greater than the force required to disengage the first ridges 16 from the circumferential groove 30 .
- the net predetermined separation force may be set at different levels for different uses of the coupling device 108 by adjusting the portion of the second ridges 116 that becomes engaged with the secondary circumferential grooves 72 as the female part 10 is rotated relative to the male part 12 .
- the net predetermined separation force may be increased by further rotating female part 10 relative to male part 12 until alignment arrow 70 aligns with the third alignment marking 82 , indicating a maximum engagement between the second ridges 116 and the secondary circumferential grooves 72 .
- a stop mechanism may be provided to prevent the further rotation of the parts 10 and 12 relative to each other, since any further rotation may be reduce the portion of the second ridges 116 engaged with the secondary circumferential grooves 72 , thereby reducing the net predetermined separation force.
- a “click” mechanism may be implemented to provide feedback to the user that alignment arrow 70 is in proper alignment with any one of or all of the first, second, or third alignment markings 78 , 80 , and 82 .
- the geometry of the inwardly tapered engagement surfaces 74 may be configured such that the inward bias of resiliently flexible arms 14 serves to push female part 10 away from male part 12 , and further configured such that the ridges 16 do not catch on the secondary circumferential grooves 72 as the parts 10 and 12 are separated.
- the coupling device 208 includes an integrated backflow prevention mechanism 90 .
- the integrated backflow prevention mechanism 90 includes a valve body 96 defining an interior chamber with an inlet and an outlet; The backflow prevention mechanism 90 ensures fluid, flow only in the direction of flow arrow 102 and substantially prevents fluid or gases from flowing in the opposite direction.
- a disk 92 is provided within the interior chamber of the valve body 96 .
- the backflow prevention mechanism 90 includes disk stand-offs 94 to prevent the disk 92 from sealing an outlet passage when fluid flows in the direction of flow arrow 102 .
- Disks stand-offs 94 may be configured to allow sufficient flow around disk 92 and between disk 92 and disk valve body 96 when disk 92 is resting upon the disk stand-offs 94 .
- the disk 92 bears against sealing surfaces 98 thereby sealing the inlet passage of the disk valve body 96 .
- Disk valve body 96 may be configured to hold a filter 100 .
- Filter 100 may be a micro-filter type filter designed to block the flow of infectious disease agents that may be potentially contained within the fluids or gases flowing through the coupling device 208 .
- Filter 100 is sealed against the valve body 96 to prevent any bypass flow.
- FIG. 7 shows a cross-sectional view of a fourth embodiment of a coupling device 308 according to the present invention.
- Coupling device 308 is provided, with a ball-type backflow prevention mechanism 110 .
- the ball-type backflow prevention mechanism 110 includes a valve body 106 having an interior chamber with an inlet and outlet, and including ball stand-offs 114 and sealing surfaces 118 .
- a ball 102 is provided within the interior chamber to ensure fluid flow only occurs in the selected direction.
- the ball-type backflow prevention mechanism. 110 may further be provided with a filter 100 , as described above.
- FIG. 8 shows a cross-sectional view of a fifth embodiment of a coupling device 408 in accordance with the present invention.
- Coupling device 408 is provided with a pinch-type backflow prevention mechanism 120 .
- the pinch-type backflow prevention. mechanism 120 includes a valve body 126 having a pinch valve 122 .
- Pinch valve 122 may be constructed of a suitable flexible resilient material that will remain closed or “pinched” in the absence of any flow in a selected direction. Flow in a direction opposite to the selected direction causes the pinch valve 122 to close. Fluid flow against the selected direction bears against the sides of the pinch valve 122 improving the seal of the valve opening.
- the pinch-type of backflow prevention mechanism 120 may be configured to allow fluids or gases to flow in the direction of flow arrow 102 and to substantially prevent fluid or gases from flowing in the opposite direction.
- Pinch valve 122 may be of modular construction.
- Pinch-type valve body 126 may be configured to seal outwardly extending flange 31 against cylindrical body 13 , as previously described, seal pinch-type valve 122 against outwardly extending flange 31 , and secure-and seal fluid line 23 as previously described. Further, valve body 126 may be configured to hold a filter 100 in a correct and sealed position, as previously described.
- FIG. 9 shows a cross-sectional view of a sixth embodiment of a coupling device 508 according to the present invention.
- the coupling device 508 includes an external med-port body 136 having a central passage 138 in fluid communication with the coupling device 508 .
- the med-port body 136 further includes a tangential passage or tube 134 providing a med-port 130 .
- External med-port 130 may be configured with a self-sealing med-port cap 132 .
- External med-port 130 may be provided to allow for needle injections or needleless injections so as to enable fluids injected through the external med-port 130 to readily mix with fluids flowing in the direction of flow arrow 102 .
- External med-port body 136 may be configured to seal outwardly extending flange 31 against cylindrical body 13 , and secure and seal fluid line 23 , as previously described.
- external med-port 130 may be provided within cylindrical body 13 of male part 12 in an alternative embodiment. It will be further appreciated that external med-port 130 may also be, configured with a backflow prevention device and/or a filter element, as previously described.
- the female and male parts 10 and 12 may be manufactured by any suitable medical-grade material, including plastics having flex characteristics that are substantially unaffected by temperature variations within a reasonable operating range.
- the parts 10 and 12 may be produced by injection molding, or any other means known in the art.
- the diaphragms 18 and 24 are not limited to a central slit 54 and may have multiple slits or other features for allowing the diaphragms 18 and 24 to remain sealed while the two parts 10 and 12 are disconnected and to open when the parts 10 and 12 are connected.
- the present invention is not limited to silicon diaphragms and may include other sealing mechanisms for ensuring the two fluid lines 22 and 23 are sealed when the two parts 10 and 12 become disengaged.
- skirt 17 portion of the sheath 19 need not be a continuous skirt, but could be made up of two or more forward projecting arms of resiliently deformable material.
- the breakaway safety feature provided by way of the snap-fit connection between the protrusions 16 and the groove 30 may be altered without affecting the function or purpose of the connection.
- the arms 14 may be arranged other than at the periphery of the cylindrical body 11 .
- the arms 14 may extend into the male part 12 and the groove 30 could be provided on the inner surface of the male part 12 .
- Other arrangements of the mechanical elements may be used to create a coupling that detaches when subjected to a predetermined separating force, for example through a magnetic coupling, a friction fit, or a semi-perforated tape or other adhesive.
Abstract
A coupling device for coupling a patient-side medical line to an equipment-side medical line. The device includes two parts, one fluidly coupled to each medical line, and each part having a seal that seals the respective medical line when the parts are disconnected. When the parts are connected, the seals unseal the medical lines so as to establish fluid communication between the medical lines. The parts are connected together by way of a coupling that detaches when subjected to a sufficient separation force. The coupling may be a snap-fit mechanism incorporating a rounded protrusion and a rounded groove that pull apart under a sufficient force. The coupling device provides for a safety breakaway feature while sealing both medical lines when disconnected.
Description
- This invention relates to medical lines and, in particular, to a coupling device for connecting two medical lines.
- Medical lines are commonly used to deliver liquids or gases to or from a patient under medical care. Medical fluid lines are used regularly in conjunction with a catheter for the intravenous (IV) delivery of fluids, often including medication. They may also be used for fluid drainage, such as in the case of a urinary catheter. Oxygen lines are often used to deliver oxygen to patients to assist in breathing.
- One of the dangers with medical fluid lines attached to a patient through a catheter is that they can become snagged or entangled on external objects or persons. This can cause the patient pain and physical damage if a medical fluid line is snagged during a fall or some other rapid movement, since the catheter may be torn from the insertion site on the patient. Alternatively, the fluid line may be torn from the IV bag or other equipment to which it is attached. In either case, spillage of body fluids or medicaments or the contamination of the fluid lines are significant risks.
- Another danger arises in the use of IV lines with newborns and infants. In some cases, infants can be strangled by IV lines if the child becomes entangled in the IV line. This danger also arises in the case of medical lines for the delivery of gases, such as oxygen lines.
- There are existing two-part connectors for coupling medical fluid lines, however these connectors fail to adequately address the problems noted above. Existing two-part connectors-are designed to lock together until manually detached by a nurse. For example, U.S. Pat. Nos. 5,549,577 and 5,122,123 and US Patent Publication Nos. 20030032940 and 200200123724, each contemplate a threaded attachment or a bayonet-style attachment which are intended to lock the connector into place.
- U.S. Pat. Nos. 4,533,349 and 5,637,088 describe connectors or fluid lines that can become detached as a result of a longitudinal pulling force, but detachment results in spillage of fluids and risk of contamination.
- Accordingly, a need exists for a coupling device for medical lines that, in part, addresses the shortcomings described above.
- The present invention provides a coupling device with a safety breakaway feature. In particular, the present invention provides a coupling device having two parts that couple together to connect two medical lines and that automatically decouple when subjected to a predetermined separating force.
- In one embodiment, the parts are connected together by way of a detachable snap-fit mechanism that separates when subjected to a predetermined longitudinal force. In a further embodiment, the parts each include a sealing mechanism for sealing the medical lines when the parts are decoupled.
- In one aspect, the present invention provides a coupling device for coupling a patient-side medical line to an equipment-side medical line. The coupling device includes a first part adapted to be coupled to a first medical line, the first part having a first passage therethrough to provide fluid communication with the first medical line, the first part including a first seal having a sealed position and an unsealed position, wherein the first seal seals the first medical line when in the sealed position, and a second part adapted to be coupled to a second medical line, the second part having a second passage therethrough to provide fluid communication with the second medical line, the second part including a second seal having a sealed position and an unsealed position, wherein the second seal seals the second medical line when in the sealed position. The parts include a connector detachably connecting the first part to the second part in a longitudinal direction, wherein the connector detaches the first and second parts in response to a predetermined force in the longitudinal direction, and wherein each of the seals moves from the sealed position to the unsealed position when the first part is detachably connected to the second part.
- In another aspect, the present invention provides a coupling device for coupling a patient-side medical line to an equipment-side medical line. The coupling device includes a first body having a first passage therethrough for coupling to a first medical line, a second body having a second passage therethrough for coupling to a second medical line, and a connection means for detachably connecting the first body-to the second body and providing fluid communication between the first and second medical lines, the connection means disconnecting the first body from the second body in response to a separating force. The first body includes a first sealing means for sealing the first medical line and the second body includes a second sealing means for sealing the second medical line when the first and second bodies are disconnected, and for unsealing the first and second medical lines when the first and second bodies are connected.
- In yet another aspect, the present provides a first adapter for a coupling to a second adapter of a coupling device for coupling a patient-side medical line to an equipment-side medical line, the second adapter having a second body adapted to be coupled to a second medical line. The first adapter includes a first body adapted to be coupled to a first medical line, the first body having a first passage therethrough to provide fluid communication with the first medical line, the first body including a first seal having a sealed position and an unsealed position, wherein the first seal seals the first medical line when in the sealed position, the first body including a connector for detachably connecting the first body to the second body in a longitudinal direction, the connector detaching the first and second bodies in response to a predetermined force in the longitudinal direction, wherein each of the seals moves from the sealed position to the unsealed position when the first body is detachably connected to the second body.
- In one embodiment, the connector connecting the first part or body to the second part or body includes a snap-fit connector comprising a ridge and a corresponding groove. In another embodiment, the snap-fit connector comprises a first ridge and a first corresponding groove and a second ridge and a second corresponding groove, wherein the second ridge is selectably engagable with the second corresponding groove so as to allow a user to select between two or more predetermined detachment forces.
- In yet other embodiments, the present invention may include a backflow prevention mechanism or valve, and may include an external med-port.
- Other aspects and features of the present invention will become apparent to those ordinarily skilled in the art upon review of the following description of specific embodiments of the invention in conjunction with the accompanying figures.
- Reference will now be made, by way of example, to the accompanying drawings which show an embodiment of the present invention, and in which:
-
FIG. 1 shows a perspective view of a coupling device according to the present invention in a disconnected state; -
FIG. 2 shows a cross-sectional view of the coupling device shown inFIG. 1 taken along the line 2-2, with the device in a disconnected state; -
FIG. 3 shows a cross-sectional view of the coupling device shown inFIG. 1 taken along the line 2-2, with the device in a connected state; -
FIG. 4 shows a close-up of the cross-sectional view of one of the diaphragms shown inFIG. 2 ; -
FIG. 5 shows a perspective view of another embodiment of a coupling device according to the present invention, in a disconnected state; -
FIG. 6 shows a cross-sectional view of a third embodiment of a coupling device according to the present invention; -
FIG. 7 shows a cross-sectional view of a fourth embodiment of a coupling device according to the present invention; -
FIG. 8 shows a cross-sectional view of a fifth embodiment of a coupling device according to the present invention; and -
FIG. 9 shows a cross-sectional view of a sixth embodiment of a coupling device according to the present invention. - Similar numerals are used in different figures to denote similar components.
- Reference is first made to
FIGS. 1 and 2 , which show an embodiment of acoupling device 8, according to the present invention, in a disconnected state. Thecoupling device 8 includes a first, or female,part 10 and a second, or male,part 12. Theparts parts parts - The
female part 10 has acylindrical body 11 having anaxial passage 20 extending through thebody 11. At the distal end of thebody 11, thepassage 20 is in fluid communication with afluid line 22. Thefluid line 22 may be coupled to thepassage 20 through any number of mechanisms for securing thefemale part 10 to thefluid line 22, including a barbed connector, crimping, a threaded coupling, a bayonet-style coupling, or a fused connection. Thepart 10 may, in one embodiment, include a bayonet termination for insertion directly into an IV solution bag to provide fluid communication with thepassage 22. In one embodiment, thefemale part 10 and/or themale part 12 are not secured directly to the fluid lines. In this embodiment, theparts - Extending forward from the proximal end of the
body 11 is anaxial tube 15 in fluid communication with thepassage 20. Theaxial tube 15 may be integrally formed with thecylindrical body 11 and terminates in anouter end 17. Theouter end 17 of the tube is sealed with afirst diaphragm 18. Accordingly, thefirst diaphragm 18 also seals thepassage 20 and thefluid line 22, thereby preventing fluid flow into or out of thefluid line 22. In one embodiment, thediaphragm 18 includes a pre-cut central slit, whereby thediaphragm 18 spreads open at the pre-cut central slit when subjected to sufficient pressure. - The
female part 10 also includes a plurality of forward extendingarms 14 arranged at the periphery of thecylindrical body 11. Thearms 14 may be integrally formed with thecylindrical body 11. The outer ends of some of thearms 14 include aridge 16 formed on the inner surface of thearms 14. As can be seen inFIG. 1 , theridge 16 may extend circumferentially along the inner surface of one ormore arms 14. Thearms 14 are resiliently flexible such that when bent radially outwards they will exert an inward radial bias. - The
male part 12 has acylindrical body 13 having anaxial chamber 26 extending longitudinally therethrough. A needle 24 (or a tube, a cannula, or other fluid line connector) is coupled to afluid line 23 and inserted into theaxial chamber 26. In one embodiment, theneedle 24 andfluid line 23 are secured to the cylindrical body. 13 by a threadedcoupler 25 having an external thread on its outer surface that cooperates with a corresponding thread formed upon the inner surface of theaxial chamber 26 to secure thecoupler 25 to thecylindrical body 13. Other mechanisms for coupling thefluid line 23 andneedle 24 to thebody 13 will be understood by those of ordinary skill in the art, and may include friction fit, adhesives, fusing, etc. - The
male part 12 further includes atubular sheath 19 disposed within theaxial chamber 26. Thesheath 19 envelopes theneedle 24 and includes a base having an outwardly extendingflange 31. The outwardly extendingflange 31 is pinched between thecylindrical body 13 and the threadedcoupler 25 such that thesheath 19 is in sealed fluid communication with theneedle 24. - The tip of the
sheath 19 terminates in asecond diaphragm 28 that seals the tip of thetubular sheath 19. Thediaphragm 28 may be formed integrally with thesheath 19. In one embodiment, thediaphragm 28 includes a pre-cut central slit, whereby thediaphragm 28 spreads open at the pre-cut central slit when subjected to sufficient pressure. - The
sheath 19 also includes askirt 21 encircling the tubular portion of thesheath 19 and extending forwardly and outwardly within theaxial chamber 26. The outer end of theskirt 21 includes an outwardly extendingflange 27 pressed against the front surface of thecylindrical body 13 and held in place with acollar 32. Thecollar 32 may be push fit into a corresponding annular depression within the front face of thecylindrical body 13. Thecollar 32 holds the outer end of theskirt 21 in place relative to thecylindrical body 13. - The front end of the
cylindrical body 13 includes an inwardly taperedouter surface 29 and acircumferential groove 30. - When the
parts diaphragms fluid lines passage 20 or theaxial chamber 26. - Reference is now made to
FIG. 3 , which shows thecoupling device 8 ofFIGS. 1 and 2 in a connected state. - When the forward or proximal ends of the female and
male parts outer surface 29 of themale part 12 fits within thearms 14 of thefemale part 10. As theridges 16 on thearms 14 are brought into contact with the inwardly taperedouter surface 29, they are pushed outwards, flexing thearms 14 radially, until theridges 16 snap into thegroove 30. Accordingly, the twoparts - The
groove 30 and theridges 16 are rounded, such that they will disengage when subjected to a sufficient longitudinal force. This disengagement force may be set at different levels for different uses of the coupling device 8 (e.g. adults versus infants; urinary catheters versus IV lines; etc.). Examples of possible force levels include 1, 5, and 10 lbs. Such a force may arise if one of thefluid lines parts ridges 16 to bear against the rounded edge of thegroove 20, causing theridges 16 to rise out of thegroove 30 against the inward bias of the resilientlyflexible arms 14. The extent of the force required to separate the twoparts ridges 16 and thegrooves 30 and altering the flexibility of thearms 14. - It will also be seen from
FIG. 3 that when the twoparts outer end 17 of theaxial tube 15 bears against the tip of thetubular sheath 18 around the periphery of thediaphragm 28. As the twoparts outer end 17 of theaxial tube 15 pushes thesheath 19 anddiaphragm 28 back, compacting the main body of thesheath 19 towards its base. As the tubular body of thesheath 19 is pushed back, thediaphragm 28 at the tip of thesheath 19 spreads apart at its central slit point or channel, revealing theneedle 24. Both the main body of thesheath 19 and thediaphragm 28 are pushed back along the body of theneedle 24 until the fluid ports of theneedle 24 are exposed to the interior of theaxial tube 15 of thefemale part 10. - The compacting of the
sheath 19 by theaxial tube 15 is performed against the resistance of theskirt 21 portion of thesheath 19. The outer end of theskirt 21 remains fixed to the front surface of thecylindrical body 13 of themale part 12, while the inner end of theskirt 21 where it meets the main body of thesheath 19 is pushed back into theaxial chamber 26. This stretching stores a tension in theskirt 21. When theparts skirt 21 causes it to contract, drawing the body of thesheath 19 back up theaxial chamber 26, causing thesheath 19 to reassume its sealed position enveloping theneedle 24. When thesheath 19 re-envelopes theneedle 24, thediaphragm 28 reseals the tip of thesheath 19, pinching the central slit shut. - It will further be seen from
FIG. 3 that when the twoparts outer end 17 of theaxial tube 15 begins to bear upon the tip of thesheath 19 and thediaphragm 24 begins to part, the tip of theneedle 24 is brought into contact with the center of thediaphragm 18 at theouter end 17 of theaxial tube 15. Theneedle 24 exerts a pressure on thediaphragm 18, causing it to spread apart at its central slit point or channel, through which theneedle 24 is inserted. - When the
parts diaphragms needle 24 to enter theaxial tube 15 and fluid communication is established between the twofluid lines parts sheath 19 and the twodiaphragms fluid lines - Accordingly, the
coupling device 8 automatically seals the twofluid lines coupling device 8 is purposely or accidentally disconnected, thereby preventing spillage or contamination. Thecoupling device 8 also permits easy connection and disconnection of different fluid lines by providing easy sterilization and resealing capability. This allows for easy connection of a new IV line or new catheter bag to a patient. Thecoupling device 8 may also be used to provide a saline/hep lock or a med port. - Upon disconnection, in one embodiment, the
coupling device 8 provides for sufficient backpressure to trigger an alarm on a pump if one is used in association with one of the medical fluid lines. - Reference is now made to
FIG. 4 , which shows a close up of a cross-sectional view of thediaphragm 28 from themale part 12. The following description of thediaphragm 28 may also apply to thediaphragm 18 on thefemale part 10. - The
diaphragm 28 seals aninner volume 50 from anexternal environment 52. It features acentral slit 54 to allow thediaphragm 28 to spread apart when the twoparts inner volume 50 contains a fluid under pressure, such that it exerts an outward pressure on thediaphragm 28. - The
diaphragm 28 features one ormore channels 56 formed in the inner surface of thediaphragm 28 and running parallel to thecentral slit 54. In one embodiment, achannel 56 is formed on each side of thecentral slit 54. Thechannels 56 each include anangled face 58 extending from the inner surface of thediaphragm 28 into thediaphragm 28 divergently from thecentral slit 54. Thechannels 56 and thecentral slit 54 define two hingedportions 62 of thediaphragm 28 that meet at thecentral slit 54. The two hingedportions 62 of thediaphragm 28 are each connected to the main part of thediaphragm 28 at athin point 60. In another embodiment, there is a singlecircumferential channel 56 around a breakpoint. - Pressure from the fluid within the
inner volume 50 bears against the inner surface of thediaphragm 28. This pressure also bears against the angled faces 58, urging the hingedportions 62 of thediaphragm 28 to pivot about theirthin points 60, thereby compressing them together at thecentral slit 54 and improving the seal. - In one embodiment, the
diaphragms sheath 19 are all manufactured from silicon. Other suitable materials may include materials such as aliphatic hydrocarbon resins, aliphatic polyester resins, copolymers of olefins and vinyl acetate, olefin-acrylate copolymers, and chlorinated hydrocarbon resins, provided that they are sufficiently resiliently elastic. - Reference is now made to
FIG. 5 , which shows a perspective view of another embodiment of acoupling device 108, according to the present invention, in a disconnected state. Thecoupling device 108 includes a first, or female,part 10 and a second, or male,part 12, theparts parts parts - The
female part 10 includes a plurality of forward extendingarms 14 arranged at the periphery of acylindrical body 11. Onesuch arm 14 may be marked with analignment arrow 70. Thearms 14 may be integrally formed with thecylindrical body 11. The outer ends of some of thearms 14 include afirst ridge 16 and asecond ridge 116 formed on the inner surface of thearms 14. As can be seen inFIG. 5 , thefirst ridge 16 and thesecond ridge 116 extend circumferentially along the inner surface of one ormore arms 14. Thearms 14 are resiliently flexible such that when bent radially outwards they will exert an inward radial bias. - The
male part 12 includes acylindrical body 13 having an inwardly taperedengagement surface 74 at its proximal end. The proximal end of thecylindrical body 13 also includes inwardly sloped clearance surfaces 76 and acircumferential groove 30. The inwardly tapered engagement surfaces 74 define a secondarycircumferential groove 72. The secondarycircumferential groove 72 is located closer to the proximal end of thecylindrical body 13 than thecircumferential groove 30. -
Cylindrical body 13 may further include first alignment marking 78, second alignment marking 80, and third alignment marking 82. The first, second, andthird alignment markings alignment arrow 70. Thealignment markings coupling device 108, such as infant, pediatric, and adult. - It will be understood that the
alignment arrow 70 may be replicated at various intervals around the perimeter offemale part 10, and that the first, second, andthird alignment markings male part 12. Further, it will be understood that there may be fewer than or more than three distinct selectable force settings and corresponding alignment markings. - When the forward or proximal ends of the female and
male parts alignment arrow 70 aligns with the first alignment marking 78, the inwardly tapered engagement surfaces 74 and inwardly slopedclearance surface 76 of themale part 12 fit within thearms 14 of thefemale part 10. As thefirst ridges 16 on thearms 14 are brought into contact with the inwardly tapered engagement surfaces 74, preferably at a point between secondarycircumferential groove 72 andcircumferential groove 30, they are pushed outwards, flexing thearms 14 radially, until thefirst ridges 16 snap into the circumferential groove. 30. The extent of the minimum force required to separate the twoparts ridges 16 and thegroove 30 and altering the flexibility of thearms 14, as previously described. Accordingly, the twoparts - The inwardly sloped clearance surfaces 76 may be configured such that the
second ridges 116 do not contact or rest against inwardly sloped clearance surfaces 76 when the twoparts alignment arrow 70 aligned with the first alignment marking 78. - Once connected in this manner, one of the
parts alignment arrow 70 aligns with the second alignment marking 80, so as to adjust and increase the predetermined separation force. On aligning thealignment arrow 70 with the second alignment marking 80, thefirst ridges 16 on thearms 14 remain engaged with thecircumferential groove 30, ensuring that thefemale part 10 remains in a fixed longitudinal position relative tomale part 12. As theparts second ridges 116 slide into alignment with the secondarycircumferential grooves 72. The secondarycircumferential groove 72 and thesecond ridges 116 may be rounded, such that they will disengage when subjected to a sufficient incremental longitudinal separation force. The incremental longitudinal separation force may be greater than the force required to disengage thefirst ridges 16 from thecircumferential groove 30. The net predetermined separation force may be set at different levels for different uses of thecoupling device 108 by adjusting the portion of thesecond ridges 116 that becomes engaged with the secondarycircumferential grooves 72 as thefemale part 10 is rotated relative to themale part 12. - The net predetermined separation force may be increased by further rotating
female part 10 relative tomale part 12 untilalignment arrow 70 aligns with the third alignment marking 82, indicating a maximum engagement between thesecond ridges 116 and the secondarycircumferential grooves 72. A stop mechanism may be provided to prevent the further rotation of theparts second ridges 116 engaged with the secondarycircumferential grooves 72, thereby reducing the net predetermined separation force. Further, a “click” mechanism may be implemented to provide feedback to the user thatalignment arrow 70 is in proper alignment with any one of or all of the first, second, orthird alignment markings - If the net disengagement force applied to the
parts first ridge 16 to bear against the rounded edge of thecircumferential groove 30, and the rounded edges of thesecond ridges 116 to bear against the rounded edges of the secondarycircumferential grooves 72, causing the first andsecond ridges grooves 30 and 71, respectively. The geometry of the inwardly tapered engagement surfaces 74 may be configured such that the inward bias of resilientlyflexible arms 14 serves to pushfemale part 10 away frommale part 12, and further configured such that theridges 16 do not catch on the secondarycircumferential grooves 72 as theparts - Reference is now made to
FIG. 6 , which shows a third embodiment of acoupling device 208 according to the present invention. Thecoupling device 208 includes an integratedbackflow prevention mechanism 90. The integratedbackflow prevention mechanism 90 includes avalve body 96 defining an interior chamber with an inlet and an outlet; Thebackflow prevention mechanism 90 ensures fluid, flow only in the direction offlow arrow 102 and substantially prevents fluid or gases from flowing in the opposite direction. Adisk 92 is provided within the interior chamber of thevalve body 96. Thebackflow prevention mechanism 90 includes disk stand-offs 94 to prevent thedisk 92 from sealing an outlet passage when fluid flows in the direction offlow arrow 102. Disks stand-offs 94 may be configured to allow sufficient flow arounddisk 92 and betweendisk 92 anddisk valve body 96 whendisk 92 is resting upon the disk stand-offs 94. When fluid flow opposesflow arrow 102, thedisk 92 bears against sealingsurfaces 98 thereby sealing the inlet passage of thedisk valve body 96. -
Disk valve body 96 may be configured to hold afilter 100.Filter 100 may be a micro-filter type filter designed to block the flow of infectious disease agents that may be potentially contained within the fluids or gases flowing through thecoupling device 208.Filter 100 is sealed against thevalve body 96 to prevent any bypass flow. - Reference is now made to
FIG. 7 which shows a cross-sectional view of a fourth embodiment of acoupling device 308 according to the present invention.Coupling device 308 is provided, with a ball-typebackflow prevention mechanism 110. The ball-typebackflow prevention mechanism 110 includes avalve body 106 having an interior chamber with an inlet and outlet, and including ball stand-offs 114 and sealing surfaces 118. Aball 102 is provided within the interior chamber to ensure fluid flow only occurs in the selected direction. The ball-type backflow prevention mechanism. 110 may further be provided with afilter 100, as described above. - Reference is now made to
FIG. 8 , which shows a cross-sectional view of a fifth embodiment of acoupling device 408 in accordance with the present invention.Coupling device 408 is provided with a pinch-typebackflow prevention mechanism 120. The pinch-type backflow prevention.mechanism 120 includes avalve body 126 having apinch valve 122. Pinchvalve 122 may be constructed of a suitable flexible resilient material that will remain closed or “pinched” in the absence of any flow in a selected direction. Flow in a direction opposite to the selected direction causes thepinch valve 122 to close. Fluid flow against the selected direction bears against the sides of thepinch valve 122 improving the seal of the valve opening. The pinch-type ofbackflow prevention mechanism 120 may be configured to allow fluids or gases to flow in the direction offlow arrow 102 and to substantially prevent fluid or gases from flowing in the opposite direction. - Pinch
valve 122 may be of modular construction. Pinch-type valve body 126 may be configured to seal outwardly extendingflange 31 againstcylindrical body 13, as previously described, seal pinch-type valve 122 against outwardly extendingflange 31, and secure-andseal fluid line 23 as previously described. Further,valve body 126 may be configured to hold afilter 100 in a correct and sealed position, as previously described. - Reference is now made to
FIG. 9 which shows a cross-sectional view of a sixth embodiment of acoupling device 508 according to the present invention. Thecoupling device 508 includes an external med-port body 136 having acentral passage 138 in fluid communication with thecoupling device 508. The med-port body 136 further includes a tangential passage ortube 134 providing a med-port 130. External med-port 130 may be configured with a self-sealing med-port cap 132. External med-port 130 may be provided to allow for needle injections or needleless injections so as to enable fluids injected through the external med-port 130 to readily mix with fluids flowing in the direction offlow arrow 102. External med-port body 136 may be configured to seal outwardly extendingflange 31 againstcylindrical body 13, and secure and sealfluid line 23, as previously described. - It will be appreciated that the features and functions of external med-
port 130 may be provided withincylindrical body 13 ofmale part 12 in an alternative embodiment. It will be further appreciated that external med-port 130 may also be, configured with a backflow prevention device and/or a filter element, as previously described. - The female and
male parts parts - In some embodiments the
diaphragms central slit 54 and may have multiple slits or other features for allowing thediaphragms parts parts - In some embodiments the present invention is not limited to silicon diaphragms and may include other sealing mechanisms for ensuring the two
fluid lines parts - In some embodiments the
skirt 17 portion of thesheath 19 need not be a continuous skirt, but could be made up of two or more forward projecting arms of resiliently deformable material. - The breakaway safety feature provided by way of the snap-fit connection between the
protrusions 16 and thegroove 30 may be altered without affecting the function or purpose of the connection. For example, thearms 14 may be arranged other than at the periphery of thecylindrical body 11. Thearms 14 may extend into themale part 12 and thegroove 30 could be provided on the inner surface of themale part 12. Other arrangements of the mechanical elements may be used to create a coupling that detaches when subjected to a predetermined separating force, for example through a magnetic coupling, a friction fit, or a semi-perforated tape or other adhesive. - Although the above embodiments have been described in association with medical fluid lines, the present invention is not limited to fluid lines and may be used in connection with other medical lines, such as oxygen lines.
- Other modifications or adaptations will be apparent to those of ordinary skill in the art.
- The present invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. Therefore, the above discussed embodiments are considered to be illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.
Claims (24)
1. A coupling device for coupling a patient-side medical line to an equipment-side medical line, said coupling device comprising:
a first part adapted to be coupled to a first medical line, said first part having a first passage therethrough to provide fluid communication with said first medical line, said first part including a first seal having a sealed position and an unsealed position, wherein said first seal seals said first medical line when in said sealed position; and
a second part adapted to be coupled to a second medical line, said second part having a second passage therethrough to provide fluid communication with said second medical line, said second part including a second seal having a sealed position and an unsealed position, wherein said second seal seals said second medical line when in said sealed position,
wherein said parts include a connector detachably connecting said first part to said second part in a longitudinal direction, wherein said connector detaches said first and second parts in response to a predetermined force in said longitudinal direction, and wherein each of said seals moves from said sealed position to said unsealed position when said first part is detachably connected to said second part.
2. The coupling device claimed in claim 1 , wherein said connector includes a snap-fit connector.
3. The coupling device claimed in claim 1 , wherein said connector includes a rounded protrusion on said first part and a cooperating groove formed in the surface of said second part.
4. The coupling device claimed in claim 3 , wherein said first part includes one or more resiliently flexible arms extending longitudinally and having formed thereon one or more of said protrusions.
5. The coupling device claimed in claim 4 , wherein said first part includes a cylindrical body, said arms are disposed around the periphery of said cylindrical body, and said protrusions extend radially inwards, and wherein said second part includes a cylindrical main body and said cooperating groove extends circumferentially within the outer surface of said cylindrical main body.
6. The coupling device claimed in claim 1 , wherein at least one of said seals includes diaphragm.
7. The coupling device claimed in claim 6 , wherein said diaphragm is formed from silicone.
8. The coupling device claimed in claim 6 , wherein said diaphragm includes a slit therethrough, and wherein in said sealed position said diaphragm pinches said slit closed, and in said unsealed position said diaphragm draws apart at said slit.
9. The coupling device claimed in claim 8 , wherein said diaphragm has an inner surface and includes a pair of channels formed within said surface on either side of said slit.
10. The coupling device claimed in claim 9 , wherein said channels are parallel to said slit, and wherein said channels each include an angled face having a surface angled with respect to said slit.
11. The coupling device claimed in claim 8 , wherein said diaphragm has an inner surface and includes a circumferential channel formed within said surface around said slit.
12. The coupling device claimed in claim 11 , wherein said circumferential channel includes an angled face having a surface angled with respect to said slit.
13. The coupling device claimed in claim 1 , wherein said second part includes a fluid delivery device disposed within said second passage and coupled to said second medical line, and wherein said second seal includes a resiliently deformable sheath enveloping said fluid delivery device.
14. The coupling device claimed in claim 13 , wherein said fluid delivery device includes a needle.
15. The coupling device claimed in claim 14 , wherein the end of said sheath includes a diaphragm having a slit therein.
16. The coupling device claimed in claim 13 , wherein said sheath includes a resiliently flexible forward extending skirt having an outer end coupled to the second part.
17. A coupling device for coupling a patient-side medical fine to an equipment-side medical line, said coupling device comprising:
a first body having a first passage therethrough for coupling to a first medical line;
a second body having a second passage therethrough for coupling to a second medical line; and
a connection means for detachably connecting said first body to said second body and providing fluid communication between said first and second medical lines, said connection means disconnecting said first body from said second body in response to a separating force;
wherein said first body includes a first sealing means for sealing said one medical line and wherein said second body includes a second sealing means for sealing said other medical line when said first and second bodies are disconnected, and for unsealing said first and second medical lines when said first and second bodies are connected.
18. The coupling device claimed in claim 14 , wherein said connection means includes a snap-fit mechanism.
19. The coupling device claimed in claim 14 , wherein said first body includes a protrusion for pushing said second sealing means into an unsealed position when said first and second bodies are connected.
20. The coupling device claimed in claim 14 , wherein said second body includes a protrusion for pushing said first sealing means into an unsealed position when said first and second bodies are connected.
21. The coupling device claimed in claim 14 , wherein said second sealing means includes a sheath means for enveloping a needle, and wherein said sheath means includes a forward extending skirt means for biasing said sheath means into a sealed position.
22. A first adapter for coupling to a second adapter of a coupling device for coupling a patient-side medical line to an equipment-side medical line, said second adapter having a second body adapted to be coupled to a first medical line, said first adapter comprising:
a first body adapted to be coupled to a second medical line, said first body having a first passage therethrough to provide fluid communication with said second medical line, said first body including a first seal having a sealed position and an unsealed position, wherein said first seal seals said second medical line when in said sealed position, said first body including a connector for detachably connecting said first body to said second body in a longitudinal direction, said connector detaching said first and second bodies in response to a predetermined force in said longitudinal direction,
wherein each of said seals moves from said sealed position to said unsealed position when said first body is detachably connected to said second body.
23. The first adapter claimed in claim 18 , wherein said connector Includes a snap-fit connector.
24. The first adapted claimed in claim 18 , wherein at least one of said seals includes a diaphragm having a slit therein.
Priority Applications (1)
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US10/564,113 US20070066965A1 (en) | 2003-07-14 | 2004-06-28 | Coupling device for medical lines |
Applications Claiming Priority (5)
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US10/619,325 US20050015075A1 (en) | 2003-07-14 | 2003-07-14 | Coupling device for medical lines |
US51461503P | 2003-10-28 | 2003-10-28 | |
PCT/CA2004/000960 WO2005004974A1 (en) | 2003-07-14 | 2004-06-28 | Coupling device for medical lines |
US10/564,113 US20070066965A1 (en) | 2003-07-14 | 2004-06-28 | Coupling device for medical lines |
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US20070066965A1 true US20070066965A1 (en) | 2007-03-22 |
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US10/564,113 Abandoned US20070066965A1 (en) | 2003-07-14 | 2004-06-28 | Coupling device for medical lines |
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US20070083156A1 (en) * | 2005-10-06 | 2007-04-12 | Atrium Medical Corporation | Subcutaneous needle connection system |
US20080171992A1 (en) * | 2006-10-12 | 2008-07-17 | Jamie Glen House | Devices for connecting catheter assembly to collection receptacle |
US7410481B1 (en) * | 2004-04-06 | 2008-08-12 | Mitts Cheryl A | Urethral catheter device and method of using |
US20090243283A1 (en) * | 2006-05-04 | 2009-10-01 | Isotopen Technologien Munchen Ag | System and Method for Closed, Drip-Free and Secure Transfer of Fluids |
US20100004618A1 (en) * | 2008-07-03 | 2010-01-07 | BAXTER INTERNATIONAL INC. and BAXTER HEALTHCARE S.A., WALLISELLEN | Port assembly for use with needleless connector |
US20100004619A1 (en) * | 2008-07-03 | 2010-01-07 | Baxter International Inc. | Port assembly for use with needleless connector |
US20100049160A1 (en) * | 2008-08-19 | 2010-02-25 | Baxter Healthcare S.A. | Port assembly for use with needleless connector |
US20100292674A1 (en) * | 2009-05-14 | 2010-11-18 | Baxter International Inc. | Needleless Connector with Slider |
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- 2004-06-28 US US10/564,113 patent/US20070066965A1/en not_active Abandoned
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US7410481B1 (en) * | 2004-04-06 | 2008-08-12 | Mitts Cheryl A | Urethral catheter device and method of using |
US20140364813A1 (en) * | 2004-12-08 | 2014-12-11 | Roche Diagnostics International Ag | Adapter for injection appliance |
US10888664B2 (en) * | 2004-12-08 | 2021-01-12 | Roche Diabetes Care, Inc. | Adapter for an injection appliance |
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US8372058B2 (en) * | 2006-05-04 | 2013-02-12 | Isotopen Technologien Munchen Ag | System and method for closed, drip-free, and secure transfer of fluids |
US20090243283A1 (en) * | 2006-05-04 | 2009-10-01 | Isotopen Technologien Munchen Ag | System and Method for Closed, Drip-Free and Secure Transfer of Fluids |
US7601142B2 (en) * | 2006-10-12 | 2009-10-13 | Colorado Catheter Company, Inc. | Devices for connecting catheter assembly to collection receptacle |
US20080171992A1 (en) * | 2006-10-12 | 2008-07-17 | Jamie Glen House | Devices for connecting catheter assembly to collection receptacle |
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US10722616B2 (en) * | 2008-02-14 | 2020-07-28 | Kci Licensing, Inc. | Devices and methods for treatment of damaged tissue |
US20180177925A1 (en) * | 2008-02-14 | 2018-06-28 | Kci Licensing, Inc. | Devices And Methods For Treatment Of Damaged Tissue |
US20100004618A1 (en) * | 2008-07-03 | 2010-01-07 | BAXTER INTERNATIONAL INC. and BAXTER HEALTHCARE S.A., WALLISELLEN | Port assembly for use with needleless connector |
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US7905873B2 (en) | 2008-07-03 | 2011-03-15 | Baxter International Inc. | Port assembly for use with needleless connector |
US20100004619A1 (en) * | 2008-07-03 | 2010-01-07 | Baxter International Inc. | Port assembly for use with needleless connector |
US8062280B2 (en) | 2008-08-19 | 2011-11-22 | Baxter Healthcare S.A. | Port assembly for use with needleless connector |
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WO2011045196A1 (en) * | 2009-10-15 | 2011-04-21 | Lucio Gibertoni | Medical device for applying catheters, particularly for thoracentesis procedures |
US8684331B2 (en) * | 2011-05-11 | 2014-04-01 | Bioflo, Llc | Valve for regulating the flow of a liquid |
US20120286185A1 (en) * | 2011-05-11 | 2012-11-15 | Spolski Kevin J | Valve for Regulating the Flow of A Liquid |
US11802627B2 (en) | 2011-05-11 | 2023-10-31 | Bioflo, Llc | Valve for regulating the flow of a liquid |
US20140163529A1 (en) * | 2012-12-10 | 2014-06-12 | Indiana University Research & Technology Corporati | Adapter For A Feeding Tube |
US9649484B2 (en) | 2013-03-28 | 2017-05-16 | Covidien Lp | Snap connection for two tubes |
US10267445B2 (en) * | 2014-03-28 | 2019-04-23 | Craig Alan Ira | Releasable valved coupler |
US20170363240A1 (en) * | 2014-03-28 | 2017-12-21 | Eldon James Corp. | Releasable Valved Coupler |
US10864362B2 (en) | 2015-08-13 | 2020-12-15 | Site Saver, Inc. | Breakaway medical tubing connector |
US10655768B2 (en) | 2015-08-13 | 2020-05-19 | Site Saver, Inc. | Breakaway connector |
US10539243B2 (en) * | 2015-08-14 | 2020-01-21 | Dana Canada Corporation | Anti-drain valve assembly with integrated fixation function |
US20180078753A1 (en) * | 2016-09-21 | 2018-03-22 | Avasys, Llc | Sterile connection access system for fluid fittings |
US10537727B2 (en) * | 2016-09-21 | 2020-01-21 | Avasys, Llc | Sterile connection access system for fluid fittings |
US10857343B2 (en) | 2017-04-06 | 2020-12-08 | Becton, Dickinson And Company | Medical devices with visual and tactile indicators |
USD835269S1 (en) * | 2017-04-06 | 2018-12-04 | Becton, Dickinson And Company | Syringe tip with indicator |
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US11123533B2 (en) * | 2017-06-27 | 2021-09-21 | B. Braun Melsungen Ag | Medical fluid connection device |
USD851759S1 (en) | 2018-01-17 | 2019-06-18 | Site Saver, Inc. | Breakaway connector for medical lines |
USD972132S1 (en) * | 2019-01-10 | 2022-12-06 | Hubiomed Inc. | Hemostasis valve |
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US20230092208A1 (en) * | 2020-03-06 | 2023-03-23 | B. Braun Melsungen Ag | Coupling element for a closed fluid transfer system, counter coupling element for a coupling element of this type, and coupling system |
US20230226340A1 (en) * | 2020-06-24 | 2023-07-20 | Cyto365 Ab | A closed-system type female connector, a method for manufacture, and a stopcock having such female connectors |
WO2024009085A1 (en) * | 2022-07-05 | 2024-01-11 | Clinisupplies Limited | A catheter bag and connections and accessories therefor |
Also Published As
Publication number | Publication date |
---|---|
ATE526055T1 (en) | 2011-10-15 |
AU2004255369B2 (en) | 2010-04-15 |
AU2004255369A1 (en) | 2005-01-20 |
WO2005004974A1 (en) | 2005-01-20 |
CA2531422A1 (en) | 2005-01-20 |
CA2531422C (en) | 2012-04-10 |
EP1644072A1 (en) | 2006-04-12 |
EP1644072B1 (en) | 2011-09-28 |
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Owner name: B & D RESEARCH AND DEVELOPMENT INC., CANADA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:WRIGHT, BRIDGET ADELE;COAMBS, DAVID JOHN;REEL/FRAME:017631/0289 Effective date: 20060308 |
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